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. 2018 Jun 14;26(9):1272–1281. doi: 10.1038/s41431-018-0187-2

Fig. 1.

Fig. 1

Schematic representation of disease-causing HNRNPK mutations on the NM_002140.4 transcript. Introns (lines), coding exons (in black), and non-coding exons (in white) are represented. Published loss-of-function mutations (below) and missense mutation (above) and new mutations (above) are indicated. The scale bar represents 100 base pairs